ZMP
ENSDARG00000053731
Ensembl ID:
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17443 | Nonsense | Available for shipment | Available now |
sa14143 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17443
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075814 | Nonsense | 7 | 252 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 25540641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 25880858 |
GRCz11 | 1 | 26574572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATATTTCTTGTGCTCTTCTGTGWCGCAGACTTGTATCTGAAGGGCCCAT[T/A]GCTGGGACGACGTGGATTTGGCTCTGTGTTTGCTGGGGTCCGCAGGTCTG
Long Flanking Sequence:
TGTTTGTTTTTATTCTTTAAAACAATTATAATAATGAAAACTGCAGAGTTGCTCAATAAAAACTGCAAGTTCCTTGTGAAAGTGTGATATAAGTGAGCAGTAAAAGTGTTTGCTGTGTGTGATTTATATTTGAGCCTCAAGCCATTCCAGACCCAGGAGAGCTGCTTTCACCCAGACAGAAGCTTTGGACACAGACACACGGGATGGCACCGCTGAGCTTCCTGGATATTTGGCTTCTCTGCCTTCACATTTGGCCGATTCTTCACCACAGATCAGAGGAACAGCAAGAGGAAAAGGCAAAGCAGCAGCCAGCAAACACCGTCCACCTCTTCCCGGAGACCGGCCAAACGCACTTGCAGAGGTCAGCACAGCTCAAGTCTTCCAGATCTTATGGCTCTGTTAGGAAATGATTTGTCATTGAAGACACTGCAGCATGTTTTCTCTTCTCTCTATATTTCTTGTGCTCTTCTGTGTCGCAGACTTGTATCTGAAGGGCCCAT[T/A]GCTGGGACGACGTGGATTTGGCTCTGTGTTTGCTGGGGTCCGCAGGTCTGATGGACTTTCAGTAAGAGATCTTCTTCCCTCCTTCATTCAGACATGCTATAGAAATGTTGCTGTCAGTTAATGTCATGTGTCTCAATCAGGCAGGTGTGATTTACTCTGTCTTTTCTGTCTGCAGGTGGCCATCAAGTACGTGTCAAAGGACCGGACCCCCGAGAGACTGAGAGTTGTGTGCTTTGGTGTGAGTCTGTGGTGTTTGATTCAGTCCTGGATATAATGGAGGGTTTGTCCTGCAGGACGGTCAGGGTTGGCTGCCGCTGGAGGTGGCATTGATGACCCCCGTCACTTCAGCTCCTGTCTGCCCCAGTGTCCTGCAGCTTCTGGACTGGTTTGACCGTGCCAGATGCTACATCTTGATCCTGGAGCGTCCGGAGCAATCCTTGCCAACATCTCCAGAGCTTCTGTGAGGAGGACGGCTGTCTGGACGAGCGTCTGGCTAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14143
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075814 | Essential Splice Site | 164 | 252 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 25539983)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 25880200 |
GRCz11 | 1 | 26573914 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCGGCTGTGGAGATCTGCWGAAGCACTCGGCCTACAAATACTTTGAAGG[T/C]GGGTTTGAGTTACAGAAGGAAACGTTCTGTTTATTATTGTGAACGTCTAC
Long Flanking Sequence:
TGTCTTTTCTGTCTGCAGGTGGCCATCAAGTACGTGTCAAAGGACCGGACCCCCGAGAGACTGAGAGTTGTGTGCTTTGGTGTGAGTCTGTGGTGTTTGATTCAGTCCTGGATATAATGGAGGGTTTGTCCTGCAGGACGGTCAGGGTTGGCTGCCGCTGGAGGTGGCATTGATGACCCCCGTCACTTCAGCTCCTGTCTGCCCCAGTGTCCTGCAGCTTCTGGACTGGTTTGACCGTGCCAGATGCTACATCTTGATCCTGGAGCGTCCGGAGCAATCCTTGCCAACATCTCCAGAGCTTCTGTGAGGAGGACGGCTGTCTGGACGAGCGTCTGGCTAAGGAAGTGCTGGTGCAGCTGATCGCGGCACTGAAACACTGCGAGAGCCGCGGACGTCAAGCCAGAGAACCTGCTGATCTCCACAGAGTCCCCGGACATCAAGCTGCTGGACTTCGGCTGTGGAGATCTGCTGAAGCACTCGGCCTACAAATACTTTGAAGG[T/C]GGGTTTGAGTTACAGAAGGAAACGTTCTGTTTATTATTGTGAACGTCTACTGATCAACTAAAGGGAATTTATTTGTACTGGAGCATTTGGAGCAGATGTTTGTGGTCTTCTTGTGTCTCTCAGGCACTCCTGCATACCCTCCTCCTGAGTGGTTTCGAAAACATCACTACAATGCCACTCCAGCTACAGTCTGGTCAGTAGTAGTGACGCTCTACAACACCCTGTGTGGCTGTTTCCCCTTCAGAGGCGCATGGAGGGTCATGTCCAGAAGCAGACTGACCTTCCTTAGGAGCTTGTCAACAGGTAAGAGATTCAGACACATTCAGAAATGGCGTGGCTAGCGAGCAGAAGTGTGTTGTTGTGTGTTCCTGAAGACATTGCTGTGTGTAATAGAGTGCAGTCAGCTGATTCGCTGGTGTCTCAGTGCAGCGCCGGCTGATCGGCCCAGTTTAGATGATCTTGAGCGCCATCCCTGGTTGCACTGAACAGGTGGCCAGTGA
Associated Phenotype:
Not determined